Product Details

SNP ID: rs199848335
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:37850681 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GACCTTGCAGAGCAATGCAACCTTT[A/G]TTCAGAAAATTGAAAAATGAACTGA
Phenotype: MIM: 607421
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: NME8 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016616.4	516	Silent Mutation	TTA,TTG	L48L	NP_057700.3